A NEW BIOCHEMICAL MODEL OF HOMEOPATHIC EFFICACY IN PATIENTS WITH CHRONIC DISEASES

Abstract

According to a contemporary model of homeopathic function, photons detected from remedies with an
associated magnetic vector potential and demonstrable frequencies in the MHz-region probably excite
substrate-enzyme-complexes along pathological pathways in patients. Substrates in high potencies regulate
these pathways as well as their reversible and irreversible inhibitors in XMK or LMK potencies, in chronic
diseases. Hashimoto disease could be cured by using the highly-potentized inhibitors of calcium metabolism
such as Platinum metallicum, Silicea and Alumina by affecting a reaction chain involved in regulating
the immune system. Furthermore, when the substrates of the thyroid enzyme metabolism are given in
high potencies, such as Kalium iodatum, Iodium, TSH, Thyroxine, Triiodo-thyroninum in XMK potency
administered twice a week, thyroid antibodies vanished after three to four months. When the symptom
of a dry cough is present, it indicates two different biochemical pathways: firstly, the respiration chain
enzymes, and secondly, the nerve-muscle-system leading to paralysis may be involved. A case of cough
associated with a lack of iron in the respiratory chain was initially healed by the inhibitors Kalium cyanicum
LMK and Hydrocyanicum acidum LMK, followed by the substrates of the respiratory chain: Ferrum
metallicum LMK, Cuprum metallicum LMK and Coenzyme Q LMK. A case of paralysis of the chest
muscles in asthmatic cough was cured by the irreversible inhibitor of acetylcholine receptor Naja tripudians
LMK, the reversible inhibitors Belladonna LMK or Atropinum XMK and by the substrate Acetylcholine
XMK. Paralyses concerning the destruction of the membranes were healed by Tetanotoxinum LMK as
an irreversible inhibitor, Lecithinum LMK as an associated substrate as well as other unsaturated fatty acids
such as EPA LMK. Potent remedies of the enzyme acetylcholinesterase were Dendroaspis LMK as an
irreversible inhibitor, Alumina LMK as a reversible inhibitor and Acetylcholin XMK as a substrate.
These results lead to the conclusion that remedies associated with irreversible inhibitors act to counteract
the syphilitic miasm, reversible inhibitors the sycotic miasm, and substrates the psora miasm. This explains
the symptom pictures of Psora, Sycosis and Syphilis in biochemical terms. If the pathological pathways
are known, the most appropriate remedies might be found to act as substrates, reversible and irreversible
inhibitors of the known biochemical pathways.